Resumo O objetivo deste trabalho foi selecionar e multiplicar clones de café Conilon (Coffea canephora Pierre ex Froehner) para obtenção de variedades clonais mais produtivas e de melhor qualidade. Foram selecionadas 267 plantas matrizes cujos parâmetros de seleção foram: produtividade, incidência de ferrugem (Hemileia vastatrix Berk et Br.) e mancha manteigosa (Colletotrichum sp.), arquitetura e vigor das plantas, tamanho e época da maturação dos frutos. Os clones selecionados foram avaliados em quatro experimentos, na Fazenda Experimental de Marilândia, pertencente ao INCAPER, em Marilândia, ES. O ensaio foi instalado em Latossolo Vermelho-Amarelo, no espaçamento de 3,5 m entre linhas e 1,5 m entre covas. Utilizou-se o delineamento de blocos casualizados, com quatro repetições e seis plantas por parcela. Dos clones selecionados, numa primeira fase, foram lançadas as primeiras variedades clonais de café Conilon, para o Estado do Espírito Santo, denominadas EMCAPA 8111, EMCAPA 8121 e, EMCAPA 8131, de ciclo de maturação precoce, médio e tardio, respectivamente, e com produtividades média de quatro colheitas oscilando entre 58 e 60 sacas de 60 kg, superando em até 33% a produtividade da testemunha.Termos para indexação: Coffea canephora, clones, propagação vegetativa, produtividade, melhoramento vegetal. Clonal varieties of Conilon coffee for the Espírito Santo State, BrazilAbstract The objective of this study was to select and to multiply clones of Conilon coffee (Coffea canephora Pierre ex Froehner) to obtain clonal varieties with improved yield and quality. Two hundred and sixty seven mother plants were selected based on coffee grain yield, rust (Hemilea vastatrix) resistance, brown blight (Colletotrichum sp.) resistance, plant architecture, plant vigor, fruit size and time to fruit maturity. The selected clones were evaluated in four field experiments conducted on a Dark Yellow Latosol (Oxisol) at Instituto Capixaba de Pesquisa, Assistência Técnica e Extensão Rural (INCAPER), in Marilândia, ES, Brazil. Coffee trees were planted in rows 3.5 m apart with 1.5 m between plants in the rows. A randomized block design with four replications and six plants per plot was used. The selected clones, EMCAPA 8111, EMCAPA 8121, and EMCAPA 8131, early, medium and late maturity, respectively, were released for the State of Espírito Santo, Brazil. The productivity varied from 58 to 60 bags of 60 kg and was 33% greater than the control variety.

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The results presented in this work support the hypothesis that Agrobacterium-mediated transformation of sorghum is feasible, analogous to what has been demonstrated for other cereals such as rice, maize, barley and wheat. The four factors that we found most influenced transformation were: the sensitivity of immature sorghum embryos to Agrobacterium infection, the growth conditions of the donor plant, type of explant and co-cultivation medium. A major problem during the development of our protocol was a necrotic response which developed in explants after co-cultivation. Immature sorghum embryos proved to be very sensitive to Agrobacterium infection and we found that the level of embryo death after co-cultivation was the limiting step in improving transformation efficiency. The addition of coconut water to the co-cultivation medium, the use of vigorous and actively growing immature embryos and the removal of excess bacteria significantly improved the survival rate of sorghum embryos and was critical for successful transformation. Hygromycin phosphotransferase (hpt) proved to be a good selectable marker for sorghum. We also found that β-glucuronidase (GUS) activity was low in most of the transgenic plant tissues tested, although it was very high in immature inflorescences. Although promising, the overall transformation efficiency of the protocol is still low and further optimization will require particular attention to be given to the number of Agrobacterium in the inoculum and the selection of sorghum genotypes and explants less sensitive to Agrobacterium infection.

-The objective of this work was to develop a genetic transformation system for tropical maize genotypes via particle bombardment of immature zygotic embryos. Particle bombardment was carried out using a genetic construct with bar and uidA genes under control of CaMV35S promoter. The best conditions to transform maize tropical inbred lines L3 and L1345 were obtained when immature embryos were cultivated, prior to the bombardment, in higher osmolarity during 4 hours and bombarded at an acceleration helium gas pressure of 1,100 psi, two shots per plate, and a microcarrier flying distance of 6.6 cm. Transformation frequencies obtained using these conditions ranged from 0.9 to 2.31%. Integration of foreign genes into the genome of maize plants was confirmed by Southern blot analysis as well as bar and uidA gene expressions. The maize genetic transformation protocol developed in this work will possibly improve the efficiency to produce new transgenic tropical maize lines expressing desirable agronomic characteristics.

Foram estudados os efeitos da concentração de sais, doses de sacarose e freqüência de renovação do meio de cultura para o desenvolvimento de eixos embrionários de cupuaçu (Theobroma grandiflorum Schum.). Testaram-se 2 concentrações de sais MS (100 e 50%), 2 níveis de sacarose (1,5 e 3%) e 3 freqüências de renovação dos meios (sem renovação, renovação aos 30 e aos 60 dias), com os meios acrescidos de ANA (0,5 mg/L) e BAP (0,3 mg/L.), semi-solidificados com ágar 0,7% e pH 5,7. Observou-se que a utilização do meio MS na concentração de sais completa, com a adição de 3% de sacarose e renovações do meio em intervalos de 30 dias, apresentou melhor desenvolvimento dos eixos embrionários.

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Phosphorus (P) stress responsive genes have been identified and characterized, including the highaffinity phosphate transporter AtPHT1;4 from Arabidopsis thaliana. This gene encodes a membrane protein that is primarily expressed in roots under phosphorus deficiency. A 2.3-kb promoter region from AtPHT1;4 has been fused with the β-glucuronidase (GUS) encoding gene and introduced into maize via biolistic bombardment to evaluate its spatiotemporal activity in a heterologous system. AtPHT1;4::GUS expression is detected preferentially in transgenic maize roots under P deficiency. Further analysis of transgenic plants has also revealed that GUS activity is higher in roots than in leaves by about sixfold. These results demonstrate the ability of AtPHT1;4 promoter to direct expression of the reporter gene in a monocot root system under P stress. This property of AtPHT1;4 promoter makes it useful to engineer maize plants to modify the soil's rhizosphere and increase efficiency of P acquisition under P stress conditions.

In this review of coffee leaf rust (CLR) in Brazil, we report: (i) the historical introduction of CLR in Brazil and the first control measures; (ii) favorable environmental conditions and times of year for the disease; (iii) breeding methods and strategies used for developing CLR-resistant cultivars; (iv) the levels, sources, and types of CLR resistance; (v) the development of Brazilian resistant cultivars; and (vi) chemical and cultural control methods. Most plantations are cultivated with susceptible cultivars, such as those of the Catuaí and Mundo Novo groups. Brazilian research institutes have developed dozens of cultivars with different levels of resistance, and significantly increased the planting of new resistant cultivars. The main sources of CLR resistance are genotypes from Híbrido de Timor, Icatu, BA series carrying the SH3 gene, and Ethiopian wild coffees. High CLR resistance is still observed in Sarchimor and SH3-carrying genotypes. Intermediate CLR resistance is observed in Ethiopian wild coffees and in Sarchimor and Icatu derivatives, where qualitative resistance has been supplanted by races of Hemileia vastatrix. Contact, mesostemic, and systemic fungicides are used for chemical control in Brazil. CLR incidence in Brazil begins to increase after the rainy season onset in November, reaches a peak in June, and remains high until August. Thus, chemical control is typically applied from December to April.